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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 3
2007 2
2008 1
2009 4
2010 7
2011 6
2012 7
2013 6
2014 5
2015 7
2016 5
2017 9
2018 6
2019 5
2020 3
2021 8
2022 3
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Search Results

76 results
Results by year
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Page 1
Microcephaly.
Passemard S, Kaindl AM, Verloes A. Passemard S, et al. Handb Clin Neurol. 2013;111:129-41. doi: 10.1016/B978-0-444-52891-9.00013-0. Handb Clin Neurol. 2013. PMID: 23622158 Review.
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder.
Courraud J, Chater-Diehl E, Durand B, Vincent M, Del Mar Muniz Moreno M, Boujelbene I, Drouot N, Genschik L, Schaefer E, Nizon M, Gerard B, Abramowicz M, Cogné B, Bronicki L, Burglen L, Barth M, Charles P, Colin E, Coubes C, David A, Delobel B, Demurger F, Passemard S, Denommé AS, Faivre L, Feger C, Fradin M, Francannet C, Genevieve D, Goldenberg A, Guerrot AM, Isidor B, Johannesen KM, Keren B, Kibæk M, Kuentz P, Mathieu-Dramard M, Demeer B, Metreau J, Steensbjerre Møller R, Moutton S, Pasquier L, Pilekær Sørensen K, Perrin L, Renaud M, Saugier P, Rio M, Svane J, Thevenon J, Tran Mau Them F, Tronhjem CE, Vitobello A, Layet V, Auvin S, Khachnaoui K, Birling MC, Drunat S, Bayat A, Dubourg C, El Chehadeh S, Fagerberg C, Mignot C, Guipponi M, Bienvenu T, Herault Y, Thompson J, Willems M, Mandel JL, Weksberg R, Piton A. Courraud J, et al. Among authors: passemard s. Genet Med. 2021 Nov;23(11):2150-2159. doi: 10.1038/s41436-021-01263-1. Epub 2021 Aug 3. Genet Med. 2021. PMID: 34345024 Free article.
ASPM Primary Microcephaly.
Verloes A, Drunat S, Passemard S. Verloes A, et al. Among authors: passemard s. 2020 Apr 2. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2020 Apr 2. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 32239881 Free Books & Documents. Review.
STIL balancing primary microcephaly and cancer.
Patwardhan D, Mani S, Passemard S, Gressens P, El Ghouzzi V. Patwardhan D, et al. Among authors: passemard s. Cell Death Dis. 2018 Jan 19;9(2):65. doi: 10.1038/s41419-017-0101-9. Cell Death Dis. 2018. PMID: 29352115 Free PMC article. Review.
WDR62 Primary Microcephaly.
Verloes A, Ruaud L, Drunat S, Passemard S. Verloes A, et al. Among authors: passemard s. 2022 Feb 17. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2022 Feb 17. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 35188728 Free Books & Documents. Review.
Endoplasmic reticulum and Golgi stress in microcephaly.
Passemard S, Perez F, Gressens P, El Ghouzzi V. Passemard S, et al. Cell Stress. 2019 Oct 30;3(12):369-384. doi: 10.15698/cst2019.12.206. Cell Stress. 2019. PMID: 31832602 Free PMC article. Review.
Golgipathies in Neurodevelopment: A New View of Old Defects.
Rasika S, Passemard S, Verloes A, Gressens P, El Ghouzzi V. Rasika S, et al. Among authors: passemard s. Dev Neurosci. 2018;40(5-6):396-416. doi: 10.1159/000497035. Epub 2019 Mar 15. Dev Neurosci. 2018. PMID: 30878996 Free article. Review.
VIP-induced neuroprotection of the developing brain.
Passemard S, Sokolowska P, Schwendimann L, Gressens P. Passemard S, et al. Curr Pharm Des. 2011;17(10):1036-9. doi: 10.2174/138161211795589409. Curr Pharm Des. 2011. PMID: 21524251 Free PMC article. Review.
Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.
Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: passemard s. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. Mol Genet Genomic Med. 2021. PMID: 34402213 Free PMC article.
76 results